Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f2d3599fb8f8f479dba95ca9bb504884 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2027 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2018 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2054 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-32 |
filingDate |
1997-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9cb98d743db5d8d333a4d5ab2221a348 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d491173e16aac74b5fff2b7489bdccc |
publicationDate |
2005-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
CZ-295226-B6 |
titleOfInvention |
A tablet comprising as active ingredient a therapeutically effective amount of galantamine hydrobromide and a process for its preparation |
abstract |
A tablet comprising as active ingredient a therapeutically effective amount of galantamine hydrobromide (1: 1) and a pharmaceutically acceptable carrier comprising a spray-dried mixture of lactose monohydrate and microcrystalline cellulose in a weight ratio of 75:25, such as diluent and crospolyvidone or croscarmellose, as insoluble or poorly soluble crosslinked a polymer that acts as a disintegrant, wherein the carrier does not contain talc as a lubricant. A method of making such a tablet comprising the steps of: (i) dry-mixing the active ingredient, disintegrant and optionally a diluent glidant; (ii) optionally mixing the lubricant with the mixture obtained in step (i); (iii) compressing the mixture obtained in step (i) or (ii) in a dry state into a tablet; and (iv) optionally film-coating the tablet obtained in step (iii) |
priorityDate |
1996-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |